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Associate Vice President - Medical Affairs

3+ years
Not Disclosed
10 March 24, 2025
Job Description
Job Type: Full Time Education: MD/DO Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Associate Vice President - Medical Affairs
Location: Indianapolis, Indiana, United States
Category: Medical
Job Type: Full-Time, Regular
Job ID: R-79452

Company Overview:
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work to discover and deliver life-changing medicines, improve disease management, and support communities through philanthropy and volunteerism.

Compensation:
Actual compensation will depend on education, experience, skills, and geographic location. Anticipated wage:

  • $252,000 - $369,600

Organization Overview:
Lilly makes a global impact by delivering innovative medicines that help people live longer, healthier, and more active lives. Through philanthropy and volunteerism, we continually find creative ways to support the communities we serve.

Purpose:
The Associate Vice President - Medical Affairs Clinical Research Physician (CRP) applies scientific and medical expertise to support launch and commercialization efforts, ensuring the delivery of strategic, high-quality medical plans. The CRP collaborates with global Development teams, Therapeutic Area Program Phase, and Translational Medicine teams, contributing to clinical plans, protocol reviews, adverse event reporting, and regulatory documentation.

Responsibilities:

Business/Customer Support (Pre and Post Launch):

  • Address scientific information needs of customers (payers, patients, healthcare providers).
  • Lead data analyses and research to provide timely responses to customer inquiries.
  • Contribute to medical strategies for brand commercialization by collaborating with global Medical Affairs and brand teams.
  • Support business-to-business and business-to-government activities as a medical expert.
  • Assist in the development, review, and approval of promotional materials.
  • Support sales representative training and contribute to the understanding of market archetypes.
  • Lead patient journey development and moments of truth based on medical knowledge.

Scientific Data Dissemination/Exchange:

  • Ensure compliance with local laws, global policies, and compliance guidelines.
  • Address unsolicited scientific information needs of external healthcare professionals.
  • Plan symposia, advisory boards, and healthcare professional meetings.
  • Support development of scientific content and publications.
  • Maintain collaborations with scientific experts, thought leaders, and professional societies.
  • Provide medical insight for customer research and congress support.

Clinical Planning:

  • Communicate with Medical Directors and Business Unit Team Physicians/Regional Medical Leaders to align life cycle plans with customer needs.
  • Collaborate with global Development and Medical Affairs teams to ensure clinical programs address local/regional needs.
  • Represent the clinical perspective in global medical planning and strategy development.

Clinical Research/Trial Execution and Support:

  • Review informed consent documents and risk profiles.
  • Collaborate with clinical research staff on protocol design, conduct, and reporting.
  • Assist with investigator identification and site selection.
  • Support study start-up, training, and clinical trial execution.
  • Monitor patient safety and ensure compliance with corporate patient safety policies.

Regulatory Support Activities:

  • Review and develop local labeling and modifications.
  • Assist in regulatory report preparation and advisory committee hearings.
  • Support risk management planning with global teams and GPS.

Scientific/Technical Expertise and Continued Development:

  • Stay informed on trends, medical advancements, and competitor products.
  • Attend and contribute to medical congresses and scientific symposia.
  • Provide scientific training to clinical study teams.

General Responsibilities:

  • Support medical budget preparation and management.
  • Contribute to team effectiveness through coaching and constructive feedback.
  • Collaborate productively with alliance, business, and vendor partners.